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Behavioral Intervention

Choice of Pain Management for Acute Pain

N/A
Recruiting
Research Sponsored by Florida State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Being 18 and above
Be older than 18 years old
Must not have
Unable to consent because of physical or mental incapacity.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediately before to after 7 to 10-minute audio recording
Awards & highlights
No Placebo-Only Group

Summary

"This trial will study if letting patients in an orthopedic clinic waiting room choose their pain management method affects their pain relief. Participants will be randomly assigned to one of three groups: listening to a

Who is the study for?
This trial is for individuals experiencing acute pain, who are currently in an orthopedic clinic waiting room. There's no specific inclusion or exclusion criteria provided, so it appears open to patients available at the site.
What is being tested?
The study is testing if choosing a pain management intervention affects its effectiveness. Participants will be randomly assigned to listen to either a psychoeducation recording about pain, a mindfulness exercise, or choose between the two.
What are the potential side effects?
Since this trial involves non-invasive interventions like educational and mindfulness recordings, there are likely minimal to no side effects associated with participation.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am 18 years old or older.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I am unable to give consent due to physical or mental reasons.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~immediately before to after 7 to 10-minute audio recording
This trial's timeline: 3 weeks for screening, Varies for treatment, and immediately before to after 7 to 10-minute audio recording for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in Pain Unpleasantness Numeric Rating Scale
Secondary study objectives
Change in Anxiety Numeric Rating Scale
Change in Pain Intensity Numeric Rating Scale

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

4Treatment groups
Experimental Treatment
Active Control
Group I: Mindful Pain Management (randomized)Experimental Treatment1 Intervention
Group II: Choice: Mindful Pain ManagementExperimental Treatment1 Intervention
Group III: Pain Psychoeducation (randomized)Active Control1 Intervention
Group IV: Choice: Pain PsychoeducationActive Control1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Mindful Pain Management
2024
N/A
~160

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Who is running the clinical trial?

Florida State UniversityLead Sponsor
220 Previous Clinical Trials
36,255 Total Patients Enrolled
2 Trials studying Acute Pain
346 Patients Enrolled for Acute Pain
~0 spots leftby Dec 2024
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